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Distal 17p13.3 microdeletion syndrome
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Narcolepsy without cataplexy
3 associated genes
4 signs/symptoms
Distal 17p13.3 microdeletion syndrome
Narcolepsy without cataplexy

YWHAE
(UniProt - OMIM)
 HCRT
(UniProt - OMIM)
HLA-DQB1
(UniProt - OMIM)
HLA-DRB1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
YWHAE
(0.63)
HLA-DRB1


Citations in the biomedical literature:


Distal 17p13.3 microdeletion syndrome
YWHAE
Narcolepsy without cataplexy
HCRT HLA-DQB1 HLA-DRB1



Distal 17p13.3 microdeletion syndrome
Narcolepsy without cataplexy

Synonym(s):
- Distal del(17)(p13.3 )
- Distal monosomy 17p13.3
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (Orphanet):
- Rare neurologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: adolescence / young
Average age of death: normal
Type of inheritance: unknown
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
Narcolepsy without cataplexy

Very frequent
- Delirium / hallucination
- Sleep and vigilance disorders
- Somnolence / hypersomnia / parasomnia

Occasional
- Psychic / behavioural troubles


Distal 17p13.3 microdeletion syndrome

(no data available)